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Re-TREAT: Re-irradiation for Relapsed Brain Metastases (RE-TREAT)

2021年11月8日 更新者:Søren Møller、Rigshospitalet, Denmark

Re-TREAT: A Phase 2 Study of Stereotactic Re-irradiation of Relapsed Brain Metastases

The Re-TREAT study is a prospective clinical, phase 2, interventional, single-arm, multicenter trial for patients with local relapse of one or more brain metastases. Patients with recurrence of one or more brain metastases that have previously been treated with stereotactic radiosurgey (SRS) are treated with repeated SRS. The aim is to evaluate the efficacy and toxicity of salvage SRS. The primary outcome is local control of the relapsed tumor and the secondary endpoints include toxicity as evaluated by the investigator and quality of life measured as a patient reported outcome. As an exploratory endpoint, the value of advanced MRI (magnetic resonance imaging) and PET (positron emission tomography) imaging as a biomarker for prediction of response to treatment or toxicity will be studied.

調査の概要

詳細な説明

Background It is estimated that 10-20 % of patients with cancer develop brain metastases (BM) and the number is increasing due to prolonged patient survival as a result of improvements in surgery and systemic treatment. With few exceptions however, chemotherapy is not effective in treating disease within the central nervous system and therefore BM are often treated as a separate compartment independently from the rest of the disease throughout the body. Treatment modalities include surgical resection, stereotactic radiosurgery (SRS) and whole brain irradiation (WBI) or a combination.

SRS is a technique where a high dose of radiation is delivered through multiple fields, often as rotational intensity modulated radiation therapy (IMRT), where the beam is aimed at the tumor from everchanging angles, in order to minimize the dose to the surrounding tissue. In contrast to other radiation modalities, where a margin is added to the target in order to eradicate tumor cells that are not visible on imaging, SRS employs very small margins because brain metastases tend to be localized with sharp boundaries to surrounding tissue. The relative low dose absorbed by the surrounding tissue allows for delivery of the whole radiation dose to the tumor in one to three treatment sessions ('fractions'), as opposed to conventionally fractionated radiotherapy which is delivered in multiple fractions for the protection of surrounding healthy tissue.

As a whole, SRS results in high rates of local tumor control (65-90%) and low rates of toxicity (10-15%), which is usually mild. The most significant adverse event following SRS is radionecrosis, which is estimated to occur in 5-25% of patients. This is a condition which is poorly defined but is commonly used to describe a situation where the contrast enhancing area in the irradiated volume increases, often accompanied by increasing edema in the surrounding tissue. The condition may or may not cause symptoms. In cases of symptomatic, progressive radionecrosis, oral corticosteroids such as prednisolone may be needed for longer periods of time. Differentiation between relapsed metastasis and radionecrosis is notoriously difficult and represents one of the major diagnostic challenges in all of neuro-oncology. Advanced imaging techniques such as dynamic MRI (e.g. perfusion weighted images) or PET (positron emission tomography) have been used to aid in differentiation in experimental studies, but this currently remains an area of research. The development of the brain lesion over time and use of close follow-up using MRI will most often aid in interpretation of the images by the multidisciplinary team conference consisting of a radiologist, a radiation oncologist and a neurosurgeon.

There is no standard treatment in case of local tumor relapse following SRS. Patients who have not previously received WBI may be offered this, but the possible detrimental effects on neurocognition and quality of life are well documented4 and many clinicians as well as patients prefer to avoid this for as long as possible. Few patients in this category are recommended surgical resection.

Salvage SRS (repeated SRS to the same area at time of relapse) is commonly practiced at some institutions, Rigshospitalet being one of them, but the evidence to support routine use is sparse. The treatment has been evaluated only in retrospective studies. These have found high rates of local control (70-90%), but as adverse events and side effects cannot be evaluated from retrospective studies without risk of critical bias, the safety of this treatment remains to be established.

Aim of the study The Re-TREAT study is a prospective clinical, phase 2, interventional, single-arm, multicenter trial with patients with local relapse of one or more brain metastases. In the trial, they are treated with salvage SRS. The aim is to evaluate the efficacy and toxicity of salvage SRS. The primary outcome is local control of the relapsed tumor and the secondary endpoints include toxicity as evaluated by the investigator and quality of life measured as a patient reported outcome. As an exploratory endpoint, the value of advanced MRI and PET-imaging as a biomarker for prediction of response to treatment or toxicity will be studied.

研究の種類

介入

入学 (予想される)

44

段階

  • 適用できない

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究連絡先のバックアップ

研究場所

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

18年歳以上 (大人、高齢者)

健康ボランティアの受け入れ

いいえ

受講資格のある性別

全て

説明

Inclusion Criteria:

  • Brain metastases of solid tumor (carcinoma of unknown origin may be included but histological verification in case of BM alone is required)
  • Progression of previously treated lesion as decided by the multidisciplinary team conference
  • Previous single fraction SRS in area in question and dose plans must be available electronically
  • Previous single fraction SRS given > 3 months previously
  • ECOG (Eastern Cooperative Oncology Group) performance status ≤2
  • Life expectancy >3 months
  • Signed written consent.
  • Patients may have more than one recurring lesion and may also have new, untreated metastases which may be treated with standard SRS (up to a total of 4 metastases in accordance with Danish national guidelines).

Exclusion Criteria:

  • Two previous courses of radiotherapy for the same metastasis (e.g. SRS and WBRT)
  • Target lesions located in- or in proximity to eloquent brain areas that require reduction of radiotherapy dose
  • Target lesion gross tumor volume (GTV) for radiotherapy greater than 14,1 cm3 (equivalent to a sphere with a diameter of 3 cm)
  • Current or planned concomitant medical treatment that is likely to be active against brain metastases (e.g. tyrosine kinase inhibitors for EGFR-positive (epidermal growth factor receptor) non-small cell lung cancer) or that may influence interpretation of images (e.g. bevacizumab, a monoclonal antibody directed towards VEGF (vascular endothelial growth factor)) in the opinion of the investigators
  • Contraindication to magnetic resonance imaging using Gadolinium contrast enhancement (e.g. pacemaker, metallic implant or impaired renal function)
  • Rapid extracranial disease progression that in the opinion of the investigators confer a high risk of drop out from the study without evaluation scan at 3 months

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:なし
  • 介入モデル:単一グループの割り当て
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的:Treatment arm
Treatment with stereotactic radiosurgery
Repeated stereotactic radiosurgery to recurring brain metastases
他の名前:
  • SRS

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Freedom from progression of treated metastasis
時間枠:3 months post treatment
Freedom from progression of lesion size defined as stable or decreasing unidimensional measurement (longest diameter) on T1-weighted contrast enhanced magnetic resonance imaging (MRI)
3 months post treatment

二次結果の測定

結果測定
メジャーの説明
時間枠
Adverse events
時間枠:12 months
Adverse events graded using National Cancer Institute (NCI) Common Toxicity Criteria (CTC) Adverse Events (AE) version 5.0
12 months
Overall response
時間枠:3 months
Overall radiographic response of all treated lesions
3 months
Neurological status
時間枠:6 months
Neurological status assessed by NANO (neurologic assessment in neuro-oncology) scale
6 months
Time to intracranial relapse
時間枠:From date of treatment until the day of radiologically documented relapse in the brain assessed up to 12 months
Time to recurrence of treated lesion or occurrence of new lesion(s)
From date of treatment until the day of radiologically documented relapse in the brain assessed up to 12 months
Overall survival
時間枠:From date of treatment until date of death from any cause assessed up to 12 months
Overall survival from entry into study
From date of treatment until date of death from any cause assessed up to 12 months
Patient reported outcomes
時間枠:6 months
Health related quality of life measured by the FACT-Br (Functional Assessment of Cancer Therapy - Brain) questionnaire
6 months

その他の成果指標

結果測定
メジャーの説明
時間枠
Positron emission tomography using fluoro-ethyl tyrosine (FET) tracer before and after treatment
時間枠:3 months
Exploratory endpoint. The measured change in biological tumor volume (BTV) and Tmax/brain (maximal tumor activity) as compared to baseline values.
3 months
Dynamic MRI using DCE (dynamic contrast enhancement) perfusion measurement before and after treatment
時間枠:3 months
Exploratory endpoint. The measured change in tumor blood volume measurement, tumor perfusion and tumor permability (Ki) as compared to baseline values.
3 months

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

捜査官

  • 主任研究者:Søren Møller, MD, PhD、Rigshospitalet, Denmark

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (実際)

2021年7月1日

一次修了 (予想される)

2023年8月20日

研究の完了 (予想される)

2023年8月20日

試験登録日

最初に提出

2021年8月9日

QC基準を満たした最初の提出物

2021年11月8日

最初の投稿 (実際)

2021年11月19日

学習記録の更新

投稿された最後の更新 (実際)

2021年11月19日

QC基準を満たした最後の更新が送信されました

2021年11月8日

最終確認日

2021年11月1日

詳しくは

本研究に関する用語

医薬品およびデバイス情報、研究文書

米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

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